
Bulletin of the Chemical Society of Japan p. 3581 - 3586 (1988)
Update date:2022-08-05
Topics:
Okubo, Masao
Inatomi, Yoshito
Taniguchi, Naoki
Imamura, Kaori
In reactions of ArN(MgBr)2 with o-MeO- and o-halo-substituted nitrobenzenes, types and yields of products were different from those in its reactions with m- and p-substituted substrates.Condensation (leading to unsymmetrical azoxy- and azobenzenes), o-substituent replacement, and nuclear substitution took place.Relative yields of products were greatly affected by substituents and reaction conditions. o-MeO and o-F favor replacement, while o-Cl, o-Br, and o-I favor substitution.Replacement and/or substitution predominate when small molar excess of reagent and low concentration are used, while condensation predominates when large molar excess of reagent and high concentration are used, which phenomenon is mechanistically discussed.
View MoreShijiazhuang Frontierchem Co., Ltd.
Contact:+86-311-89271196
Address:4-4-202 No.15 Biandian Street,Shijiazhuang
website:http://www.shengmaochem.com
Contact:86-27-82853423, 82819281
Address:Rm 202, A Unit Huaqiao Building No. 2, Lihuangpi Road, Wuhan, China
Jiangsu Dacheng Pharmaceutical and Chemical Co.,Ltd
Contact:+86-0517-87036900
Address:Chuzhou Chemical park, Huai'an, Jiangsu Province
JIANGSU GRAND XINYI PHARMACEUTICAL CO.,LTD
website:http://www.xypharm.com/
Contact:+86-515-84383317
Address:Chenli Road,Costal Chemical Area Binhai,Yancheng, Jiangsu,China
Sichuan Highlight Fine Chemicals Co., Ltd.
Contact:+86-28-8525 1605
Address:A5-102 Airport base,388 West Airport Huang He Zhong Lu,2 Section
Doi:10.1016/S0040-4020(01)89838-0
(1988)Doi:10.1134/S1070328409110128
(2009)Doi:10.1002/zaac.200900265
(2009)Doi:10.1007/BF00486671
(1988)Doi:10.1021/jo00286a018
(1989)Doi:10.1021/jo100703b
(2010)